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Figs 15–17 in Four new feather mite species of the genus Proctophyllodes Robin (Astigmata: Proctophyllodidae) from China
Figs 15–17. Proctophyllodes garrula sp. nov., male. 15. Dorsal view. 16. Ventral view. 17. Anal sucker. Scale bars: 15–16 = 100 μm, 17 = 10 μm.
Figs 4–5 in Four new feather mite species of the genus Proctophyllodes Robin (Astigmata: Proctophyllodidae) from China
Figs 4–5. Proctophyllodes flexuosa sp. nov., female. 4. Dorsal view. 5. Ventral view. Scale bar = 100 μm.
Figs 13–14 in Four new feather mite species of the genus Proctophyllodes Robin (Astigmata: Proctophyllodidae) from China
Figs 13–14. Proctophyllodes brevis sp. nov., female. 13. Dorsal view. 14. Ventral view. Scale bar = 100 μm.
Figs 1–3 in Four new feather mite species of the genus Proctophyllodes Robin (Astigmata: Proctophyllodidae) from China
Figs 1–3. Proctophyllodes flexuosa sp. nov., male. 1. Dorsal view. 2. Ventral view. 3. Anal sucker. Scale bars: 1–2 = 100 μm, 3 = 10 μm.
Figs 10–12 in Four new feather mite species of the genus Proctophyllodes Robin (Astigmata: Proctophyllodidae) from China
Figs 10–12. Proctophyllodes brevis sp. nov., male. 10. Dorsal view. 11. Ventral view. 12. Anal sucker. Scale bars: 10–11 =
Figs 6–9 in Four new feather mite species of the genus Proctophyllodes Robin (Astigmata: Proctophyllodidae) from China
Figs 6–9. Proctophyllodes flexuosa sp. nov., male. 6. Leg I. 7. Leg II. 8. Leg III. 9. Leg IV. Scale bars = 50 μm.
Text-fig. 8. Lanfrancia subglobosa E.REID et M.CHANDLER. a–c, e–g: Holotype V. 23014. a: reflected light. b, c: Surface renderings from micro-CT data. a, b: Lateral views with dorsal surface of locule facing forward and locule casts protruding in upper part. c: Apical view. d: Fruit showing two locule casts the dorsal surfaces of which face to the left and the right, V. 30417(1). e–g: Successive digital transverse sections showing four u to v to c-shaped locules from micro-CT data. h: Physical transverse section of specimen in (d). i–k: Physical transverse section, V. 30419 from Herne Bay, blue lines in K indicating limits of fibre layer lining the locule. l: Detail from (h), showing sclerenchyma composing the septa and central axis. m: Transverse section, enlargement from (i), showing anatomy of tissues adjacent to the dorsal infold. Blue lines indicate limits of the fibre layer lining the locule. n: Part of (m) recut, tangential section transecting the dorsal infold (central), both limbs of the locule cast, and peripheral parts of the pericarp on either side. o: Detail from (n), showing anatomy of the infold. Scale bars 5 mm in (a–h) (a–g share the same bar), 3 mm in (i), 1 mm in (j–m), 0.5 mm in (n), 0.2 mm in (o). in Mastixioid Fruits (Cornales) From The Early Eocene London Clay Flora: Morphology, Anatomy And Nomenclatural Revision
Text-fig. 8. Lanfrancia subglobosa E.REID et M.CHANDLER. a–c, e–g: Holotype V. 23014. a: reflected light. b, c: Surface renderings from micro-CT data. a, b: Lateral views with dorsal surface of locule facing forward and locule casts protruding in upper part. c: Apical view. d: Fruit showing two locule casts the dorsal surfaces of which face to the left and the right, V. 30417(1). e–g: Successive digital transverse sections showing four u to v to c-shaped locules from micro-CT data. h: Physical transverse section of specimen in (d). i–k: Physical transverse section, V. 30419 from Herne Bay, blue lines in K indicating limits of fibre layer lining the locule. l: Detail from (h), showing sclerenchyma composing the septa and central axis. m: Transverse section, enlargement from (i), showing anatomy of tissues adjacent to the dorsal infold. Blue lines indicate limits of the fibre layer lining the locule. n: Part of (m) recut, tangential section transecting the dorsal infold (central), both limbs of the locule cast, and peripheral parts of the pericarp on either side. o: Detail from (n), showing anatomy of the infold. Scale bars 5 mm in (a–h) (a–g share the same bar), 3 mm in (i), 1 mm in (j–m), 0.5 mm in (n), 0.2 mm in (o).
Text-fig. 3. Juglandaceae. Carya (a–x). Scale bars = 1 cm. a–e: USNM PAL 772346. Micro-CT scan surface rendering. a, b: Lateral, c: apical, d: basal views. e: Virtual equatorial transverse section. f–n: USNM PAL 772347. f: Lateral view, reflected light, showing path of saw cut for transverse section of (i). g: Basal view, reflected light. h: Apical view, micro-CT surface rendering. i: Physical transverse section displaying locule and cellular preservation of parts of wall. j–n: Virtual sections from micro-CT scan data. j: Transverse section at apical 1/3 of nut. Note narrow lacunae (arrows). k: Longitudinal section parallel to primary septum, traversing one of the cotyledon lobes and showing secondary septum at base. l: Longitudinal section in plane at right angles to (k) in plane of primary septum, showing divergent placental bundles arising from base of nut (arrows). m: Equatorial transverse section showing two lobes of locule separated by primary septum. n: Transverse section near base of nut showing primary and secondary septa, creating four basal lobes of locule; note diverging placental bundles (arrows). o–x: USNM PAL 772351. o: Lateral view of broken nut with exposed locule cast, reflected light. p: Same orientation of nut, micro-CT surface rendering. q: Same specimen lateral view, rotated 90° from (p), micro-CT surface rendering. r: Apical view, reflected light. s–x: Virtual sections from micro-CT in The Early Middle Eocene Wagon Bed Carpoflora Of Central Wyoming, U.S.A.
Text-fig. 3. Juglandaceae. Carya (a–x). Scale bars = 1 cm. a–e: USNM PAL 772346. Micro-CT scan surface rendering. a, b: Lateral, c: apical, d: basal views. e: Virtual equatorial transverse section. f–n: USNM PAL 772347. f: Lateral view, reflected light, showing path of saw cut for transverse section of (i). g: Basal view, reflected light. h: Apical view, micro-CT surface rendering. i: Physical transverse section displaying locule and cellular preservation of parts of wall. j–n: Virtual sections from micro-CT scan data. j: Transverse section at apical 1/3 of nut. Note narrow lacunae (arrows). k: Longitudinal section parallel to primary septum, traversing one of the cotyledon lobes and showing secondary septum at base. l: Longitudinal section in plane at right angles to (k) in plane of primary septum, showing divergent placental bundles arising from base of nut (arrows). m: Equatorial transverse section showing two lobes of locule separated by primary septum. n: Transverse section near base of nut showing primary and secondary septa, creating four basal lobes of locule; note diverging placental bundles (arrows). o–x: USNM PAL 772351. o: Lateral view of broken nut with exposed locule cast, reflected light. p: Same orientation of nut, micro-CT surface rendering. q: Same specimen lateral view, rotated 90° from (p), micro-CT surface rendering. r: Apical view, reflected light. s–x: Virtual sections from micro-CT
Text-fig. 9. a–d: Nyssidium orientale SAMYLINA, Partizansk, Starosuchan Formation, Barremian, a – spec. BIN 506/3749, general view of four fruits, b1 – spec. BIN 506/3749-1, holotype, b2 – spec. BIN 506/3749-2, c – spec. BIN 506/3749-6, d – spec. BIN 506/3749-5; e–f: Cercidiphyllum sujfunense KRASSILOV, Konstantinovka, Galenki Formation, early-middle Albian, e – spec. IBSS 11-135, fruit, f – spec. IBSS 11-134, leaf, holotype. Scale bar 5 mm in a, e, f and 2 mm in b–d. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia
Text-fig. 9. a–d: Nyssidium orientale SAMYLINA, Partizansk, Starosuchan Formation, Barremian, a – spec. BIN 506/3749, general view of four fruits, b1 – spec. BIN 506/3749-1, holotype, b2 – spec. BIN 506/3749-2, c – spec. BIN 506/3749-6, d – spec. BIN 506/3749-5; e–f: Cercidiphyllum sujfunense KRASSILOV, Konstantinovka, Galenki Formation, early-middle Albian, e – spec. IBSS 11-135, fruit, f – spec. IBSS 11-134, leaf, holotype. Scale bar 5 mm in a, e, f and 2 mm in b–d.
Figs 16–23 in A new genus and four new species of Eriophyidae from China (Acari: Eriophyoidea)
Figs 16–23. Phyllocoptruta alstonia Wang, Gu & Tan, sp. nov. 16. Coxigenital area, female. 17. Female, dorsal view. 18. Empodium. 19. Male genitalia. 20. Female, lateral view. 21. Leg I. 22. Leg II. 23. Annuli, lateral view.
Figs 1–8 in A new genus and four new species of Eriophyidae from China (Acari: Eriophyoidea)
Figs 1–8. Dicoxiseta litsea Wang, Tan & Yang, sp. nov. 1. Coxigenital area, female. 2. Female, dorsal view. 3. Empodium. 4. Male genitalia. 5. Female, lateral view. 6. Leg I. 7. Leg II. 8. Annuli, lateral view.
Figs 9–15 in A new genus and four new species of Eriophyidae from China (Acari: Eriophyoidea)
Figs 9–15. Eriophyes casearius Wang, Yang & Tan, sp. nov. 9. Female, anterior dorsal view. 10. Female, antero-lateral view. 11. Coxigenital area, female. 12. Empodium. 13. Male genitalia. 14. Female, lateral view. 15. Annuli, lateral view.
Acceleration Data at Various Locations on Vehicle On Four Post Test Rig over Different Roads and at Different Tyre Pressures
<p>Dataset of acceleration data at various locations on sport utility vehicle on four post test rig over different roads and at different tyre pressures. This dataset can be used for driving comfort evaluation. </p>
Figure 1: Asymmetric representation for the ¯rst four generations, in its elec- trical equivalent-THE RESPIRATORY IMPEDANCE IN AN ASYMMETRIC MODEL OF THE LUNG STRUCTURE
<p>For example, the average of the radius ratio<br> changes from 2¡0:1713 = 0:8881 to 0:8923 when only the ¯rst 16 generations are<br> taken into account, respectively to 0:8783 for the alveoli (generations 17-24)<br> [5]. This implies that the homothety factor changes, depending on the spatial<br> location within the tree. On the other hand, if we analyze the radius ratio from<br> generations 1 to 24 in steps of 4, we obtain an average of 0:8535, whereas if we<br> use steps of 2, we obtain an average homothety factor of 0:8623. These changes<br> might not seem signi¯cant, but one should recall that they are originated by<br> the symmetric geometry of the respiratory tree. However, when asymmetry<br> is considered, one deals with several homothety factors, i.e. as schematically<br> drawn in figure 1.</p>
Figure 1: Asymmetric representation for the ¯rst four generations, in its elec- trical equivalent-THE RESPIRATORY IMPEDANCE IN AN ASYMMETRIC MODEL OF THE LUNG STRUCTURE
<p>These changes<br> might not seem signi¯cant, but one should recall that they are originated by<br> the symmetric geometry of the respiratory tree. However, when asymmetry<br> is considered, one deals with several homothety factors, i.e. as schematically<br> drawn in ¯gure 1.</p>
FIGURE 2 in Complete mitochondrial genome of four Scleromystax barbatus (Siluriformes: Callichthyidae) populations
FIGURE 2 | Phylogenetic analysis of 13 Corydoradinae and Hoplosternum littorale (Callichthyinae member) species as the outgroup based on the nucleotide sequences of 13 PCGs from the mitochondrial genome. Bootstrap values are shown next to nodes and the scale bar shows 0.03 changes. Population codes in Tab. 1.
FIGURE 1 in Complete mitochondrial genome of four Scleromystax barbatus (Siluriformes: Callichthyidae) populations
FIGURE 1 | A. Geographic location of the Scleromystax barbatus populations in coastal Atlantic Rainforest rivers. B. Male of S. barbatus. Photo by Caio Feltrin. C. Complete mitochondrial genome of S. barbatus from the AR population. Population codes in Tab. 1.
Quantifying direct and indirect effects of early-season herbivory on reproduction across four brassicaceous plant species
<div> <p>Insect herbivores can directly affect plant reproduction by feeding on reproductive tissues, or indirectly by feeding on vegetative tissues for which plants are unable to compensate. Additionally, early-arriving herbivores may have cascading effects on plant reproduction by altering the later-arriving community. However, the dynamic interplay between plant development and the assembly of herbivore communities remains underexplored. Hence, it is unclear whether non-outbreak levels of ambient herbivory early in the development of plants can impact plant fitness and to what extent these effects are mediated through changes in plant development and subsequent herbivory. By excluding the herbivore community in an exclosure experiment and by manipulating early-season herbivory in a common garden field experiment replicated across four Brassicaceae species and two years, we tested whether early-season herbivory by caterpillars (<em>Pieris rapae)</em> or aphids (<em>Myzus persicae</em>) affected development, reproduction, and the herbivore communities associated with individual plants. In addition, we tested a causal hypothesis to assess the relative importance and temporal interplay between variation in herbivore communities and variation in plant development in determining plant reproduction. Early-season herbivory affected plant reproduction in the exclosure experiment, with effects being highly dependent on the plant species, the herbivore species, and the year. However, we found no such effects in the field experiment. The exploratory path analysis indicated that variation in plant reproduction is best predicted by variation in plant development, explaining 80% of the total effect on seed production. This suggests that early-season herbivory had limited effects on later plant development, and plants were able to attenuate the impact of early-season herbivory. However, no clear compensatory mechanism could be identified. While early-season herbivory has the potential to affect plant reproduction through changes in plant development or the subsequent development of the associated community, these effects were small and varied across closely related species. This suggests that plant species may be exposed to different levels of natural selection by early-season herbivores through plant- or community-mediated effects on reproduction.</p> </div>
Fig. 13 in Taxonomic and Zoogeographic Notes on Japanese Orthocentrinae (Hymenoptera, Ichneumonidae), with Descriptions of Four New Species
Fig. 13. Megastylus (Dicolus) impressor Schiødte, 1838 (A–C: EUM, female) ― A: lateral habitus; B: head, frontal view; C: head, mesosoma, and metasoma, dorsolateral view.
Fig. 10 in Taxonomic and Zoogeographic Notes on Japanese Orthocentrinae (Hymenoptera, Ichneumonidae), with Descriptions of Four New Species
Fig. 10. Hemiphanes gravator Förster, 1871 (A–C: EUM, female; D–G: EUM, male) ― A, D: lateral habitus; B, E: head, frontal view; C, G: head, mesosoma, and metasoma, dorsal view; F: head and mesoscutum, dorsolateral view.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.